Canonical Allele Identifier: PA2830199252
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 467474

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_596869.4:p.Leu22386Phe
CA1990134
NM_133378.4:c.67156C>T